
%0 Journal Article
%A Harris, RLN 
%T The synthesis of alkyl- and aryl-substituted 1,3,5-triazines
%J Australian Journal of Chemistry
%D 1981/03/01
%V 34
%N 3
%P 623-634
%K 
%R https://doi.org/10.1071/CH9810623
%U https://www.publish.csiro.au/paper/CH9810623 
%X The reaction of chloromethyleneiminium salts with N-cyanoamidines provides a new and versatile route to alkyl- and aryl-substituted 1,3,5-triazines. Variation of substituents in the starting materials allows the synthesis of monoaryl-, diaryl-, alkyl-aryl- and certain mono- and di-alkyl-l,3,5-triazines bearing a variety of other substituents including hydrogen, chlorine and O-, S- and N-radicals. The generally good yields, ready availability of starting materials, and the scope and facility of the reaction make it the method of choice for the synthesis of 1,3,5-triazines with these substitution patterns. 
